Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Rita Soler‐Yanes"'
Autor:
Elena Buñuel, Rita Soler‐Yanes, Diego J. Cárdenas, Pablo Domingo-Legarda, M. Teresa Quirós‐López
Publikováno v:
European Journal of Organic Chemistry. 2018:4900-4904
Autor:
Manuel Guisán-Ceinos, Diego J. Cárdenas, Elena Buñuel, Iván Arribas-Álvarez, Rita Soler‐Yanes
Publikováno v:
Chemistry - A European Journal. 23:1584-1590
We describe the unprecedented formation of allenes by Ni-catalyzed cross-coupling of propargyl bromides with alkylzinc halides. The reaction regioselectivity is complementary to the previously reported formation of propargyl-coupled compounds. Experi
Autor:
Rita Soler‐Yanes, Diego J. Cárdenas, Manuel Guisán-Ceinos, Víctor Martín-Heras, Mariola Tortosa
Publikováno v:
Chemical communications (Cambridge, England). 54(60)
Herein we describe a robust and practical method to prepare enantiomerically enriched trisubstituted allenes using alkyl Grignard reagents and bench stable propargylic ammonium salts. Excellent yields as well as regio- and stereoselectivities are obs
Publikováno v:
European Journal of Organic Chemistry. 2014:6625-6629
Conditions for the fast Ni-catalyzed Kumada-type cross-coupling of functionalized benzyl and allyl chlorides with alkylmagnesium reagents were discovered. The use of Ni(acac)2–TMEDA (acac = acetylacetonate, TMEDA = N,N,N′,N′-tetramethyl-1,2-eth
Autor:
Rita Soler‐Yanes, Manuel Guisán-Ceinos, Diego J. Cárdenas, Daniel Collado-Sanz, Vilas B. Phapale, Elena Buñuel
Publikováno v:
Chemistry - A European Journal. 19:8405-8410
Suggesting novel disconnections: A powerful Ni-catalyzed cascade reaction involving cyclization followed by cross-coupling allows the formation of up to three alkyl-alkyl bonds in a single operation by using alkene-containing alkyl iodides and Grigna
Autor:
Rita, Soler-Yanes, Iván, Arribas-Álvarez, Manuel, Guisán-Ceinos, Elena, Buñuel, Diego J, Cárdenas
Publikováno v:
Chemistry (Weinheim an der Bergstrasse, Germany). 23(7)
We describe the unprecedented formation of allenes by Ni-catalyzed cross-coupling of propargyl bromides with alkylzinc halides. The reaction regioselectivity is complementary to the previously reported formation of propargyl-coupled compounds. Experi
ChemInform Abstract: Nickel-Catalyzed Kumada Coupling of Benzyl Chlorides and Vinylogous Derivatives
Publikováno v:
ChemInform. 46
The Ni(acac)-catalyzed cross-coupling reactions of benzyl chlorides with alkylmagnesium reagents is studied.
Autor:
Diego J. Cárdenas, Manuel Guisán-Ceinos, Vilas B. Phapale, Rita Soler‐Yanes, Daniel Collado-Sanz, Elena Buñuel
Publikováno v:
ChemInform. 44
A powerful Ni-catalyzed cascade reaction involving cyclization followed by cross-coupling allows the formation of up to three alkyl—alkyl bonds in a single operation by using alkene-containing alkyl iodides and Grignard reagents.